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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30642Generated: October 26, 2026

4-Nitrobenzaldehyde → 5-(4-Nitrobenzylidene)-1,3-thiazolidine-2,4-dione

https://huagongshe.com/reaction/30642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
SolventEthanolHCID 702—
Product5-(4-Nitrobenzylidene)-1,3-thiazolidine-2,4-dioneHCID 276826459.2%

Reaction Steps

A mixture of 4-nitrobenzaldehyde (15.1 g), 1,3-thiazolidine-2,4-dione (11.70 g), piperidine (1.70 g) and ethanol (300 mL) was heated under reflux for 24 hrs. The reaction mixture was concentrated. The obtained residue was washed with ethanol to give 5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione as yellow crystals (14.8 g, yield 59%). Recrystallization thereof from acetone-hexane gave pale-yellow prism crystals. melting point: 272-273° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423159B2
Source datasetuspto-grants-2008_09
ORD IDord-02854ddf1583494d8386c11c20c29345
Source noteuspto-grants-2008_09